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Edx detector

Manufactured by Bruker

The EDX detector is a specialized piece of laboratory equipment used for elemental analysis. It is designed to detect and identify the chemical elements present in a sample through the analysis of X-ray emissions. The EDX detector measures the energy of X-rays emitted by the sample, which is characteristic of the elements present, allowing for the determination of the sample's elemental composition.

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5 protocols using edx detector

1

TEM Characterization of Colloidal AgNPs

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The samples were examined in the high contrast mode on a Hitachi High-Tech HT7700 transmission electron microscope (Hitachi High-Technologies Corporation, Tokyo, Japan) at 120 kV accelerating voltage. The instrument is equipped with a Bruker EDX detector that allows elemental analysis and a SAED aperture that could be used to collect diffraction patterns directly during the sample inspection. A drop of each colloidal AgNPs solution was placed on a 300-mesh carbon-coated copper grid (Ted Pella) and vacuum-dried at room temperature for 24 h prior to examination.
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2

Structural Characterization of Nanomaterials via SEM

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SEM was used to verify that sheets and hollow cages were made and to examine their morphology. The samples were placed on a conductive carbon tape on top of an SEM stub and then dried for 24 hours in a vacuum desiccator. These samples were sputter-coated with gold and viewed under a JCM-6000 Benchtop SEM (JEOL Ltd., Japan) using a secondary electron detector with a 15-kV accelerating voltage at different magnifications. For zoom-in images, samples were coated with carbon using a sputter coater (Denton Desk V, NJ, USA) and then examined with a Zeiss GeminiSEM 500 FE-SEM (Zeiss, Jena, Germany). Objects were scanned with 1 keV and imaged by a high-efficiency secondary electron detector. In addition, to generate phosphorus density maps, EDX images were also taken using a Zeiss 1550 with a Schottky field-emission source and a nanometer-scale electron probe. A Bruker EDX detector was used, with an aperture size of 60 μm and electron beam of 7.0 kV. The Gemini objective lens uses a combined electrostatic/magnetic lens, which serves to reduce the lens aberration and improve the resolution, especially at low voltages.
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3

Microbial Carbonate Mineral Characterization

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The sediment samples collected from sabkhas, and mangrove forest had been analyzed initially to ensure the existence of high magnesium carbonate as a bulk in these sites. One g from each sediment sample was manually grounded and homogenized with a mortar and pestle, mixed evenly, and left to dry at 37 °C overnight. The dried samples were analyzed by XRD and SEM/EDS.
The minerals formed in pure bacterial cultures were extracted from the solid media. The bacterial biomass was stripped from the surface of the solid medium by slightly scraping the top layer with a sterile scalpel. The mineral crystals were washed three times with 15 mL distilled water. This process does not alter the shape of the crystals, as confirmed by optical microscopy before and after recovery [10] . The overnight dried samples at 37 °C, were analyzed by SEM/EDS and XRD techniques.
The SEM analysis was conducted utilizing a Nova Nano Scanning Electron Microscopy equipped with a Bruker EDX Detector with a magnification of 200,000X and a resolution of 5 nm. The EDS was obtained in accordance with the “ASTM standard method E1508–12a”, using a spot size of 5 and an accelerating voltage of 20 kV with an error rate of 4%. The PANalytical- multipurpose Empyrean X-ray diffractometer was used to determine the bulk mineralogical composition of the retrieved minerals.
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4

Comprehensive Characterization of Al-MnO2 Battery

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dc ionic conductivity and EIS were measured using a Novocontrol broadband dielectric/impedance spectrometer. Field-emission SEM (FESEM) images of MnO2 cathode and Al anode were obtained using a Leo 1550 Keck FESEM, in which EDX analysis was also carried out with a Bruker EDX detector. The XRD pattern of α-MnO2 cathodes during electrochemical reaction was taken with a Rigaku x-ray diffractometer. ATR-FTIR spectra of different electrolytes were obtained using a Bruker Hyperion FTIR spectrometer. XPS SSX-100 was applied to study the chemistry information of SEI on the Al surface and MnO2 cathodes. Galvanostatic measurements of Al batteries were performed using Neware battery testers at room temperature. CV diagram was performed on an electrochemical workstation of CH 600E. TEM images were obtained from the FEI Titan Themis CryoS/TEM, in which EELS spectra were obtained using a Gatan GIF Tridiem energy filter.
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5

Mineralogical Characterization of Recovered Minerals

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The recovered minerals as described in section 2.5 were subjected to SEM/EDS and XRD analysis. The SEM was performed using Nova Nano Scanning Electron Microscopy equipped with Bruker EDX Detector with 5 nm resolution and a magnification of 200,000 × . The EDS was obtained following “ASTM standard method E1508–12a”, with spot size 5 at an accelerating voltage of 20 kV and 4% error.
The bulk mineralogical composition of the recovered minerals was determined using a PANalytical- multipurpose Empyrean X-ray diffractometer. Crystal Impact MATCH! Version 3.12 Software was used for the analysis of XRD spectra and semi-quantitively determination of amounts of formed minerals in each mixture.
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